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Chemical Structure| 1289126-21-1 Chemical Structure| 1289126-21-1

Structure of 1289126-21-1

Chemical Structure| 1289126-21-1

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Product Details of [ 1289126-21-1 ]

CAS No. :1289126-21-1
Formula : C10H12O2
M.W : 164.20
SMILES Code : O=CC1=CC=C(CC)C(OC)=C1

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Application In Synthesis of [ 1289126-21-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1289126-21-1 ]

[ 1289126-21-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4433-63-0 ]
  • [ 43192-34-3 ]
  • [ 1289126-21-1 ]
YieldReaction ConditionsOperation in experiment
2 g With potassium phosphate; palladium diacetate; tricyclohexylphosphine; In water; toluene;Reflux; Inert atmosphere; To a mixture of 4-bromo-3-methoxy-benzaldeyde (5.0 g, 23.38 mmol), ethylboronic acid (5.2 g, 71 mmol) and potassium phosphate (17.3 g, 81.83 mmol) in toluene (100 mL) was added water (10 mL), tricyclohexylphosphine (0.65 g, 2.33 mmol) and palladium (II) acetate (260 mg, 1.16 mmol). The reaction mixture was heated at reflux under argon atmosphere overnight. The reaction was cooled, and then diluted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous sodium sulfate and then concentrated in vacuo. The residue was purified by column chromatography to give 4-ethyl-3-methoxy-benzaldehyde (2 g).
2 g With potassium phosphate; palladium diacetate; tricyclohexylphosphine; In water; toluene;Inert atmosphere; Reflux; Step 1: Preparation of 4-ethyl-3-methoxy-benzaldehyde To a mixture of 4-bromo-3-methoxy-benzalcleyde (5.0 g, 23.38 mmol), ethylboronic acid (5.2 g.71 mmol) and potassium phosphate (17.3 g, 81.83 mmol) in toluene ( 100 ml.) was added water ( 10 mL), tricyclohexylphosphinc (0.65 g, 2.33 mmol) and palladium (II) acetate (260 mg, 1.16 mmol). The reaction mixture was heated at reflux under argon atmosphere overnight. The reaction was cooled, and then diluted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous sodium sulfate and then concentrated in vacuo. The residue was purified by column chromatography to give 4-ethyl-3-methoxy-benzaldehydc (2 g).
 

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